8 research outputs found

    MOESM3 of Piscine orthoreovirus can infect and shed through the intestine in experimentally challenged Atlantic salmon (Salmo salar L.)

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    Additional file 3. Temporal development in relationship between PRV levels in blood and faeces of i.p. group from 7 dpc to 70 dpc. Fish from each sampling time point are marked according to legend insert Day-Group. Coloured circles indicate the approximate centre of distribution of PRV values for each sampling time point as indicated by inserted coloured text boxes. The arrows indicate potential temporal trends in PRV distribution centre in the course of the experiment

    MOESM2 of Piscine orthoreovirus can infect and shed through the intestine in experimentally challenged Atlantic salmon (Salmo salar L.)

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    Additional file 2. Temporal development in relationship between PRV levels in blood and heart of i.p. group from 7 dpc to 70 dpc. Fish from each sampling time point are marked according to legend insert Day-Group. Coloured circles indicate the approximate centre of distribution of PRV values for each sampling time point as indicated by inserted coloured text boxes. The arrows indicate potential temporal trends in PRV distribution centre in the course of the experiment

    Effects of cnidarian biofouling on salmon gill health and development of amoebic gill disease

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    <div><p>This study examines the potential implications of biofouling management on the development of an infectious disease in Norwegian farmed salmon. The hydroid <i>Ectopleura larynx</i> frequently colonises cage nets at high densities (thousands of colonies per m<sup>2</sup>) and is released into the water during regular <i>in-situ</i> net cleaning. Contact with the hydroids’ nematocysts has the potential to cause irritation and pathological damage to salmon gills. Amoebic gill disease (AGD), caused by the amoeba <i>Paramoeba perurans</i>, is an increasingly international health challenge in Atlantic salmon farming. AGD often occurs concomitantly with other agents of gill disease. This study used laboratory challenge trials to: (1) characterise the gill pathology resulting from the exposure of salmon to hydroids, and (2) investigate if such exposure can predispose the fish to secondary infections–using <i>P</i>. <i>perurans</i> as an example. Salmon in tanks were exposed either to freshly ‘shredded’ hydroids resembling waste material from net cleaning, or to authentic concentrations of free-living <i>P</i>. <i>perurans</i>, or first to ‘shredded’ hydroids and then to <i>P</i>. <i>perurans</i>. Gill health (AGD gill scores, non-specific gill scores, lamellar thrombi, epithelial hyperplasia) was monitored over 5 weeks and compared to an untreated control group.</p><p>Nematocysts of <i>E</i>. <i>larynx</i> contained in cleaning waste remained active following high-pressure cleaning, resulting in higher non-specific gill scores in salmon up to 1 day after exposure to hydroids. Higher average numbers of gill lamellar thrombi occurred in fish up to 7 days after exposure to hydroids. However, gill lesions caused by hydroids did not affect the infection rates of <i>P</i>. <i>perurans</i> or the disease progression of AGD. This study discusses the negative impacts hydroids and current net cleaning practices can have on gill health and welfare of farmed salmon, highlights existing knowledge gaps and reiterates the need for alternative approaches to net cleaning.</p></div

    Scanning electron microscope images of a hydroid tentacle and nematocysts.

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    <p>a) Close-up of a tentacle of <i>E</i>. <i>larynx</i>, showing cnidocilia of undischarged nematocysts protruding the surface, ready to discharge on contact. b) Two discharged stenotele nematocysts (identified according to Östmann et al. [<a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0199842#pone.0199842.ref038" target="_blank">38</a>]) found after triggering release with acetic acid.</p

    Descriptive and numeric scores corresponding to non-specific gill lesioning and AGD pathology, adapted from Taylor et al. [34].

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    <p>Descriptive and numeric scores corresponding to non-specific gill lesioning and AGD pathology, adapted from Taylor et al. [<a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0199842#pone.0199842.ref034" target="_blank">34</a>].</p

    Experimental schedule showing sampling events (grey arrows) and numbers of sampled fish.

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    <p>Exposure to hydroids <i>Ectopleura larynx</i> ("H") took place one day post sampling of the naïve fish; exposure to <i>Paramoeba perurans</i> ("PP") took place one day post hydroid exposure (dphe). In addition, the distribution of the four treatment groups (C = Control, H = Hydroids, PP = <i>P</i>. <i>perurans</i>, H + PP = Hydroids + <i>P</i>. <i>perurans</i>) over the eight experimental tanks is shown. The numbers of sampled fish refer to each tank during each sampling event.</p
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